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Clinical Features and Outcomes of 23 Patients with Wiskott- Aldrich Syndrome: A Single-Center Experience

Turkish journal of haematology, 2020-11, Vol.37 (4), p.271-281

2020

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Pediatric Invasive Aspergillosis: A Retrospective Review of 59 Cases

Japanese Journal of Infectious Diseases, 2022/11/30, pp.JJID.2022.346

2023

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A Novel Mutation in a Child with Atypical Wiskott-Aldrich Syndrome Complicated by Cytomegalovirus Infection

Turkish journal of haematology, 2019-02, Vol.36 (1), p.70-71

2019

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Biallelic loss-of-function mutation in NIK causes a primary immunodeficiency with multifaceted aberrant lymphoid immunity

Nature communications, 2014-11, Vol.5 (1), p.5360, Article 5360

2014

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Chronic enteropathy associated with SLCO2A1 gene and hereditary fructose intolerance: A coincidence of two rare diseases

Arab journal of gastroenterology, 2022-11, Vol.23 (4), p.290-293

2022

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Patients with Primary Immunodeficiencies in Pediatric Intensive Care Unit: Outcomes and Mortality-Related Risk Factors

Journal of clinical immunology, 2014-04, Vol.34 (3), p.309-315

2014

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Inherited DOCK2 Deficiency in Patients with Early-Onset Invasive Infections

The New England journal of medicine, 2015-06, Vol.372 (25), p.2409-2422

2015

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Astımlı Çocukların Serum D Vitamini ve Çinko Düzeyleri ile Klinik Bulguları Arasında Bir İlişki Var mı?

Ankara medical journal, 2018-12, Vol.18 (4), p.528-536

2018

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Local abscess due to BCGitis

Çocuk enfeksiyon dergisi, 2022-12, Vol.16 (4), p.297-297

2022

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BCGitis’e Bağlı Lokal Apse

Çocuk enfeksiyon dergisi, 2022-12, Vol.16 (4), p.295-295

2022

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T Regulatory Cells in Children with Atopic Dermatitis

Ankara Ueniversitesi Tip Fakültesi mecmuasi, 2018-08, Vol.71 (2), p.118-122

2018

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ST2 and Reg3α: Can they predict aGvHD, steroid refractoriness and transplant-related mortality in pediatric patients after HSCT?

Hematology, Transfusion and Cell Therapy, 2024-04

2024

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Chromosome 22q11.2 Deletion Syndrome (DiGeorge Syndrome/Velocardiofacial Syndrome)

Turkish Journal of Immunology, 2014-12, Vol.2 (3), p.57-66

Haskoloğlu, Zehra Şule

2014

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Normal mean platelet volume and thrombocytopenia: It may still be Wiskott–Aldrich syndrome

Pediatric allergy and immunology, 2024-08, Vol.35 (8), p.e14206-n/a

2024

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Does the Hyper IgM Phenotype Affect Prognosis in Ataxia Telangiectasia?

Astım allerji immünoloji, 2020-01, Vol.18 (1), p.38-46

2020

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The Determining Factors for Outcome of Pediatric Intensive Care Admitted Children After Stem Cell Transplantation

Journal of pediatric hematology/oncology, 2023-08, Vol.45 (6), p.e768-e772

2023

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Junctional Epidermolysis Bullosa Linked to Homozygous Mutation in LAMC2 Gene: A Case Report With Eosinophil-Rich Inflammatory Infiltrate

The American journal of dermatopathology, 2024-07

2024

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Pediatric Invasive Aspergillosis: a Retrospective Review of 59 Cases

Japanese Journal of Infectious Diseases, 2023/03/31, Vol.76(2), pp.113-119

2023

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Is antibiotic lock therapy effective for the implantable longterm catheter-related bloodstream infections in children?

Turkish journal of pediatrics, 2019, Vol.61 (6), p.895-904

2019

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Is There a Relationship between Clinical Symptoms of Asthmatic Children and Serum Levels of Vitamin D and Zinc?

Ankara medical journal, 2018-12

2018

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Immunoglobulin Isotype Deficiency Together with Allergic Diseases

Astım allerji immünoloji, 2016-12, Vol.14 (3), p.164-169

2016

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A Clinical Approach to a Child with Hypoalbuminemia and Lymphopenia

Journal of clinical immunology, 2016-05, Vol.36 (4), p.370-373

2016

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Lymphoproliferation, Autoimmunity, and Recurrent Infections: Which Primary Immunodeficiency?

Turkish Archives of Pediatrics, 2024-01, Vol.59 (1), p.106-108

2024

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Clinical Features and Outcomes of 23 Patients with Wiskott- Aldrich Syndrome: A Single-Center Experience

Pediatric Invasive Aspergillosis: A Retrospective Review of 59 Cases

A Novel Mutation in a Child with Atypical Wiskott-Aldrich Syndrome Complicated by Cytomegalovirus Infection

Biallelic loss-of-function mutation in NIK causes a primary immunodeficiency with multifaceted aberrant lymphoid immunity

Chronic enteropathy associated with SLCO2A1 gene and hereditary fructose intolerance: A coincidence of two rare diseases

Patients with Primary Immunodeficiencies in Pediatric Intensive Care Unit: Outcomes and Mortality-Related Risk Factors

Risks and outcomes of invasive fungal infections in pediatric allogeneic hematopoietic stem cell transplant recipients receiving fluconazole prophylaxis: a multicenter cohort study by the Turkish Pediatric Bone Marrow Transplantation Study Group

Inherited DOCK2 Deficiency in Patients with Early-Onset Invasive Infections

Astımlı Çocukların Serum D Vitamini ve Çinko Düzeyleri ile Klinik Bulguları Arasında Bir İlişki Var mı?

Local abscess due to BCGitis

BCGitis’e Bağlı Lokal Apse

T Regulatory Cells in Children with Atopic Dermatitis

ST2 and Reg3α: Can they predict aGvHD, steroid refractoriness and transplant-related mortality in pediatric patients after HSCT?

Chromosome 22q11.2 Deletion Syndrome (DiGeorge Syndrome/Velocardiofacial Syndrome)

Normal mean platelet volume and thrombocytopenia: It may still be Wiskott–Aldrich syndrome

Does the Hyper IgM Phenotype Affect Prognosis in Ataxia Telangiectasia?

The Determining Factors for Outcome of Pediatric Intensive Care Admitted Children After Stem Cell Transplantation

Junctional Epidermolysis Bullosa Linked to Homozygous Mutation in LAMC2 Gene: A Case Report With Eosinophil-Rich Inflammatory Infiltrate

Pediatric Invasive Aspergillosis: a Retrospective Review of 59 Cases

Is antibiotic lock therapy effective for the implantable longterm catheter-related bloodstream infections in children?

Is There a Relationship between Clinical Symptoms of Asthmatic Children and Serum Levels of Vitamin D and Zinc?

Immunoglobulin Isotype Deficiency Together with Allergic Diseases

Combined immunodeficiency and Epstein-Barr virus-induced B cell malignancy in humans with inherited CD70 deficiency

A Clinical Approach to a Child with Hypoalbuminemia and Lymphopenia

Lymphoproliferation, Autoimmunity, and Recurrent Infections: Which Primary Immunodeficiency?

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